Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.05.001
Syuhaidah Abu Bakar , Suresh Kumar , Kok-Keong Loke , Hoe-Han Goh , Normah Mohd Noor
Mangosteen (Garcinia mangostana Linn.) is an ultra-tropical tree characterized by its unique dark purple fruits with white flesh. The xanthone-rich purple pericarp tissue contains valuable compounds with medicinal properties. Following previously reported genome sequencing of a common variety of mangosteen [1], we performed another whole genome sequencing of a commercially popular variety of this fruit species (var. Mesta) for comparative analysis of its genome composition. Raw reads of the DNA sequencing project were deposited to SRA database with the accession number SRX2709728.
{"title":"DNA shotgun sequencing analysis of Garcinia mangostana L. variety Mesta","authors":"Syuhaidah Abu Bakar , Suresh Kumar , Kok-Keong Loke , Hoe-Han Goh , Normah Mohd Noor","doi":"10.1016/j.gdata.2017.05.001","DOIUrl":"10.1016/j.gdata.2017.05.001","url":null,"abstract":"<div><p>Mangosteen (<em>Garcinia mangostana</em> Linn.) is an ultra-tropical tree characterized by its unique dark purple fruits with white flesh. The xanthone-rich purple pericarp tissue contains valuable compounds with medicinal properties. Following previously reported genome sequencing of a common variety of mangosteen <span>[1]</span>, we performed another whole genome sequencing of a commercially popular variety of this fruit species (var. Mesta) for comparative analysis of its genome composition. Raw reads of the DNA sequencing project were deposited to SRA database with the accession number SRX2709728.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 118-119"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.05.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35005012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.03.011
Yong Huang, Xiao Chan Gao, Jian Li Xiong, Hong Tao Ren, Xi Hong Sun
Next-generation technologies for determination of genomics and transcriptomics composition have a wide range of applications. Andrias davidianus, has become an endangered amphibian species of salamander endemic in China. However, there is a lack of the molecular information. In this study, we obtained the RNA-Seq data from a pool of A. davidianus tissue including spleen, liver, muscle, kidney, skin, testis, gut and heart using Illumina HiSeq 2500 platform. A total of 15,398,997,600 bp were obtained, corresponding to 102,659,984 raw reads. A total of 102,659,984 reads were filtered after removing low-quality reads and trimming the adapter sequences. The Trinity program was used to de novo assemble 132,912 unigenes with an average length of 690 bp and N50 of 1263 bp. Unigenes were annotated through number of databases. These transcriptomic data of A. davidianus should open the door to molecular evolution studies based on the entire transcriptome or targeted genes of interest to sequence. The raw data in this study can be available in NCBI SRA database with accession number of SRP099564.
{"title":"Sequencing and de novo transcriptome assembly of the Chinese giant salamander (Andrias davidianus)","authors":"Yong Huang, Xiao Chan Gao, Jian Li Xiong, Hong Tao Ren, Xi Hong Sun","doi":"10.1016/j.gdata.2017.03.011","DOIUrl":"https://doi.org/10.1016/j.gdata.2017.03.011","url":null,"abstract":"<div><p>Next-generation technologies for determination of genomics and transcriptomics composition have a wide range of applications. <em>Andrias davidianus</em>, has become an endangered amphibian species of salamander endemic in China. However, there is a lack of the molecular information. In this study, we obtained the RNA-Seq data from a pool of <em>A. davidianus</em> tissue including spleen, liver, muscle, kidney, skin, testis, gut and heart using Illumina HiSeq 2500 platform. A total of 15,398,997,600<!--> <!-->bp were obtained, corresponding to 102,659,984 raw reads. A total of 102,659,984 reads were filtered after removing low-quality reads and trimming the adapter sequences. The Trinity program was used to de novo assemble 132,912 unigenes with an average length of 690<!--> <!-->bp and N50 of 1263<!--> <!-->bp. Unigenes were annotated through number of databases. These transcriptomic data of <em>A. davidianus</em> should open the door to molecular evolution studies based on the entire transcriptome or targeted genes of interest to sequence. The raw data in this study can be available in NCBI SRA database with accession number of SRP099564.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 109-110"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.03.011","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92030635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.04.003
Mohd Razik Midin , Kok-Keong Loke , Maria Madon , Mohd Shukor Nordin , Hoe-Han Goh , Normah Mohd Noor
The “Queen of Fruits” mangosteen (Garcinia mangostana L.) produces commercially important fruits with desirable taste of flesh and pericarp rich in xanthones with medicinal properties. To date, only limited knowledge is available on the cytogenetics and genome sequences of a common variety of mangosteen (Abu Bakar et al., 2016 [1]). Here, we report the first single-molecule real-time (SMRT) sequencing data from whole genome sequencing of mangosteen of Mesta variety. Raw reads of the SMRT sequencing project can be obtained from SRA database with the accession numbers SRX2718652 until SRX2718659.
“水果女王”山竹(Garcinia mangostana L.)生产具有商业价值的重要果实,具有令人满意的果肉味道和富含药用特性的山酮的果皮。迄今为止,关于山竹常见品种的细胞遗传学和基因组序列的知识有限(Abu Bakar et al., 2016[1])。在此,我们报告了Mesta山竹品种全基因组测序的首个单分子实时(SMRT)测序数据。SMRT测序项目的原始reads可从SRA数据库获得,登录号为SRX2718652至SRX2718659。
{"title":"SMRT sequencing data for Garcinia mangostana L. variety Mesta","authors":"Mohd Razik Midin , Kok-Keong Loke , Maria Madon , Mohd Shukor Nordin , Hoe-Han Goh , Normah Mohd Noor","doi":"10.1016/j.gdata.2017.04.003","DOIUrl":"https://doi.org/10.1016/j.gdata.2017.04.003","url":null,"abstract":"<div><p>The “Queen of Fruits” mangosteen (<em>Garcinia mangostana</em> L.) produces commercially important fruits with desirable taste of flesh and pericarp rich in xanthones with medicinal properties. To date, only limited knowledge is available on the cytogenetics and genome sequences of a common variety of mangosteen (Abu Bakar et al., 2016 <span>[1]</span>). Here, we report the first single-molecule real-time (SMRT) sequencing data from whole genome sequencing of mangosteen of Mesta variety. Raw reads of the SMRT sequencing project can be obtained from SRA database with the accession numbers SRX2718652 until SRX2718659.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 134-135"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.04.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92077598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Roseomonas sp. strain TAS13 isolated from an activated sludge sample degrades N-acylhomoserine lactones (AHLs) that are widely utilized as a signal in bacterial quorum sensing systems. The draft genome of Roseomonas sp. TAS13 contains 816 contigs (total 5,078,941 bp) which carries 4760 protein-coding genes and 52 tRNA genes (DDBJ/EMBL/GenBank accession numbers BDLP01000001 through BDLP01000816).
{"title":"Novel quorum quenching enzymes identified from draft genome of Roseomonas sp. TAS13","authors":"Eri Nasuno , Tomohiro Suzuki , Ryoko Suzuki , Chigusa Okano , Takeshi Kurokura , Ken-ichi Iimura , Norihiro Kato","doi":"10.1016/j.gdata.2017.02.001","DOIUrl":"10.1016/j.gdata.2017.02.001","url":null,"abstract":"<div><p><em>Roseomonas</em> sp. strain TAS13 isolated from an activated sludge sample degrades <em>N</em>-acylhomoserine lactones (AHLs) that are widely utilized as a signal in bacterial quorum sensing systems. The draft genome of <em>Roseomonas</em> sp. TAS13 contains 816 contigs (total 5,078,941<!--> <!-->bp) which carries 4760 protein-coding genes and 52 tRNA genes (DDBJ/EMBL/GenBank accession numbers BDLP01000001 through BDLP01000816).</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 22-23"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.02.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34796481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.03.003
Hui Zhang , Gilbert Audira , Yuan Li , Weiwei Xian , Muhammed Muhsin Varikkodan , Chung-Der Hsiao
The contraction and relaxation events of the muscle is mediated by the coordination of many important calcium cycling proteins of ryanodine receptor (RYR), troponin C (TNNC), parvalbumin (PVALB), sarcoendoplasmic reticulum calcium transport ATPase (SERCA) and calsequestrin (CASQ). In higher vertebrates, the expression level of calcium cycling proteins are positively correlated to the muscle contraction/relaxation ability of the cell. In this study, we used RNAseq to explore the expression profile of calcium cycling genes between two marine fish of Bombay duck (Harpadon nehereus) and beltfish (Trichiurus lepturus) with poor and robust swimming activities, respectively. We have studied the hypothesis whether the expression level of calcium cycling proteins are also positive correlated to swimming ability in fish. We used Illumina sequencing technology (NextSeq500) to sequence, assemble and annotate the muscle transcriptome of Bombay duck for the first time. A total of 47,752,240 cleaned reads (deposited in NCBI SRA database with accession number of SRX1706379) were obtained from RNA sequencing and 26,288 unigenes (with N50 of 486 bp) were obtained after de novo assembling with Trinity software. BLASTX against NR, GO, KEGG and eggNOG databases show 100%, 65%, 26%, 94% and 88% annotation rate, respectively. Comparison of the dominantly expressed unigenes in fish muscle shows calcium cycling gene expression in beltfish (SRX1674471) is 1.4- to 51.6-fold higher than Bombay duck. Among five calcium cycling genes, the fold change results are very significant in CASQ (51.6 fold) and PVALB (9.1 fold) and both of them are responsive for calcium binding to reduce free calcium concentration in the sarcoendoplasmic reticulum and cytoplasm. In conclusion, we confirmed that the high abundant expression rate of calcium cycling genes in robust swimming fish species. The current muscle transcriptome and identified calcium cycling gene data can provide more insights into the muscle physiology of fish.
{"title":"Comparative study the expression of calcium cycling genes in Bombay duck (Harpadon nehereus) and beltfish (Trichiurus lepturus) with different swimming activities","authors":"Hui Zhang , Gilbert Audira , Yuan Li , Weiwei Xian , Muhammed Muhsin Varikkodan , Chung-Der Hsiao","doi":"10.1016/j.gdata.2017.03.003","DOIUrl":"10.1016/j.gdata.2017.03.003","url":null,"abstract":"<div><p>The contraction and relaxation events of the muscle is mediated by the coordination of many important calcium cycling proteins of ryanodine receptor (RYR), troponin C (TNNC), parvalbumin (PVALB), sarcoendoplasmic reticulum calcium transport ATPase (SERCA) and calsequestrin (CASQ). In higher vertebrates, the expression level of calcium cycling proteins are positively correlated to the muscle contraction/relaxation ability of the cell. In this study, we used RNAseq to explore the expression profile of calcium cycling genes between two marine fish of Bombay duck (<em>Harpadon nehereus</em>) and beltfish (<em>Trichiurus lepturus</em>) with poor and robust swimming activities, respectively. We have studied the hypothesis whether the expression level of calcium cycling proteins are also positive correlated to swimming ability in fish. We used Illumina sequencing technology (NextSeq500) to sequence, assemble and annotate the muscle transcriptome of Bombay duck for the first time. A total of 47,752,240 cleaned reads (deposited in NCBI SRA database with accession number of SRX1706379) were obtained from RNA sequencing and 26,288 unigenes (with N50 of 486<!--> <!-->bp) were obtained after de novo assembling with Trinity software. BLASTX against NR, GO, KEGG and eggNOG databases show 100%, 65%, 26%, 94% and 88% annotation rate, respectively. Comparison of the dominantly expressed unigenes in fish muscle shows calcium cycling gene expression in beltfish (SRX1674471) is 1.4- to 51.6-fold higher than Bombay duck. Among five calcium cycling genes, the fold change results are very significant in CASQ (51.6 fold) and PVALB (9.1 fold) and both of them are responsive for calcium binding to reduce free calcium concentration in the sarcoendoplasmic reticulum and cytoplasm. In conclusion, we confirmed that the high abundant expression rate of calcium cycling genes in robust swimming fish species. The current muscle transcriptome and identified calcium cycling gene data can provide more insights into the muscle physiology of fish.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 58-61"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.03.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34884037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.05.005
Ali Amiri , Toomaj Sabooteh , Farhad Shahsavar , Khatereh Anbari , Flora Pouremadi
Objective
Tuberculosis (TB) is caused by infection of Mycobacterium tuberculosis. Host genetic variability is an important determinant of the risk of developing TB in humans. Although the association between MBL polymorphisms and TB has been studied in various populations, the results are controversial. The aim of this study was to investigate mannose-binding lectin (MBL) gene polymorphisms with susceptibility to pulmonary tuberculosis (PTB) in a Lur population of Iran.
Methods
In this case-control study, four functional MBL gene polymorphisms (HL, XY, PQ and AB) were genotyped by using PCR Single Strand Conformation Polymorphism (SSCP) technique in a Lur population living in Lorestan Province, consisting of 100 patients with pulmonary tuberculosis (PTB) age and sex matched 100 healthy controls (HCs). Association analyses were performed with the SPSS 21 statistical software.
Results
We found that MBL (HH) genotype polymorphism significantly was associated with increased susceptibility to TB (35% in patients vs. 22% in controls, P = 0.0417, OR = 1.909, %95 CI = 1.020–3.573). Additionally, H allele showed a significant association with increased risk of TB (56.5% in patients vs. 46% in controls, P = 0.0357, OR = 1.525, %95 CI = 1.028–2.262). Also, the distribution of L allele in patients was significantly lower frequency in TB patients compared to controls (43.5% vs. 54%, P = 0.0357, OR = 0.656, %95 CI = 0.442–0.973). However, the allelic and genotypic frequencies of AB, XY and PQ polymorphisms were not significantly different between the patients and the controls. We couldn't detect any significant differences between haplotypes among TB patients and healthy controls.
Conclusions
Our findings demonstrated that HH genotype and H allele may increase the susceptibility to pulmonary TB in the Lur population of Iran, although L allele may decrease the susceptibility to pulmonary TB in this population. We suggest that it is necessary to further more studies with larger sample size and other ethnic population.
目的结核(TB)是由结核分枝杆菌感染引起的疾病。宿主遗传变异是人类发生结核病风险的一个重要决定因素。尽管在不同人群中研究了MBL多态性与结核病之间的关系,但结果存在争议。本研究的目的是研究甘露糖结合凝集素(MBL)基因多态性与伊朗鲁尔人群肺结核(PTB)易感性的关系。方法采用PCR单链构象多态性(SSCP)技术,对100例年龄和性别与100例健康对照(hc)相匹配的洛雷斯坦省鲁尔族肺结核(PTB)患者的4种MBL基因多态性(HL、XY、PQ和AB)进行基因分型。采用SPSS 21统计软件进行关联分析。结果MBL (HH)基因型多态性与TB易感性增加显著相关(患者35% vs对照组22%,P = 0.0417, OR = 1.909, %95 CI = 1.020-3.573)。此外,H等位基因与结核病风险增加显著相关(患者为56.5%,对照组为46%,P = 0.0357, OR = 1.525, %95 CI = 1.028-2.262)。此外,L等位基因在结核病患者中的分布频率显著低于对照组(43.5% vs. 54%, P = 0.0357, OR = 0.656, %95 CI = 0.442-0.973)。而AB、XY和PQ多态性的等位基因和基因型频率在患者和对照组之间无显著差异。我们没有发现结核病患者和健康对照之间的单倍型有任何显著差异。结论HH基因型和H等位基因可能增加伊朗鲁尔人群对肺结核的易感性,而L等位基因可能降低该人群对肺结核的易感性。我们建议有必要进一步开展更大样本量和其他民族人群的研究。
{"title":"Mannose-Binding Lectin (MBL) gene polymorphisms in susceptibility to pulmonary tuberculosis among the Lur population of Lorestan Province of Iran","authors":"Ali Amiri , Toomaj Sabooteh , Farhad Shahsavar , Khatereh Anbari , Flora Pouremadi","doi":"10.1016/j.gdata.2017.05.005","DOIUrl":"10.1016/j.gdata.2017.05.005","url":null,"abstract":"<div><h3>Objective</h3><p>Tuberculosis (TB) is caused by infection of Mycobacterium tuberculosis. Host genetic variability is an important determinant of the risk of developing TB in humans. Although the association between <em>MBL</em> polymorphisms and TB has been studied in various populations, the results are controversial. The aim of this study was to investigate mannose-binding lectin (<em>MBL</em>) gene polymorphisms with susceptibility to pulmonary tuberculosis (PTB) in a Lur population of Iran.</p></div><div><h3>Methods</h3><p>In this case-control study, four functional <em>MBL</em> gene polymorphisms (<em>HL</em>, <em>XY</em>, <em>PQ</em> and <em>AB</em>) were genotyped by using PCR Single Strand Conformation Polymorphism (SSCP) technique in a Lur population living in Lorestan Province, consisting of 100 patients with pulmonary tuberculosis (PTB) age and sex matched 100 healthy controls (HCs). Association analyses were performed with the SPSS 21 statistical software.</p></div><div><h3>Results</h3><p>We found that <em>MBL</em> (<em>HH</em>) genotype polymorphism significantly was associated with increased susceptibility to TB (35% in patients vs. 22% in controls, P<!--> <!-->=<!--> <!-->0.0417, OR<!--> <!-->=<!--> <!-->1.909, %95 CI<!--> <!-->=<!--> <!-->1.020–3.573). Additionally, <em>H</em> allele showed a significant association with increased risk of TB (56.5% in patients vs. 46% in controls, P<!--> <!-->=<!--> <!-->0.0357, OR<!--> <!-->=<!--> <!-->1.525, %95 CI<!--> <!-->=<!--> <!-->1.028–2.262). Also, the distribution of <em>L</em> allele in patients was significantly lower frequency in TB patients compared to controls (43.5% vs. 54%, P<!--> <!-->=<!--> <!-->0.0357, OR<!--> <!-->=<!--> <!-->0.656, %95 CI<!--> <!-->=<!--> <!-->0.442–0.973). However, the allelic and genotypic frequencies of <em>AB</em>, <em>XY</em> and <em>PQ</em> polymorphisms were not significantly different between the patients and the controls. We couldn't detect any significant differences between haplotypes among TB patients and healthy controls.</p></div><div><h3>Conclusions</h3><p>Our findings demonstrated that <em>HH</em> genotype and <em>H</em> allele may increase the susceptibility to pulmonary TB in the Lur population of Iran, although <em>L</em> allele may decrease the susceptibility to pulmonary TB in this population. We suggest that it is necessary to further more studies with larger sample size and other ethnic population.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 146-150"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.05.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35023907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Here, we present the draft genome (377.3 Mbp) of Corchorus olitorious cv. JRO-524 (Navin), which is a leading dark jute variety developed from a cross between African (cv. Sudan Green) and indigenous (cv. JRO-632) types. We predicted from the draft genome a total of 57,087 protein-coding genes with annotated functions. We identified a large number of 1765 disease resistance-like and defense response genes in the jute genome. The annotated genes showed the highest sequence similarities with that of Theobroma cacao followed by Gossypium raimondii. Seven chromosome-scale genetically anchored pseudomolecules were constructed with a total size of 8.53 Mbp and used for synteny analyses with the cocoa and cotton genomes. Like other plant species, gypsy and copia retrotransposons were the most abundant classes of repeat elements in jute. The raw data of our study are available in SRA database of NCBI with accession number SRX1506532. The genome sequence has been deposited at DDBJ/EMBL/GenBank under the accession LLWS00000000, and the version described in this paper will be the first version (LLWS01000000).
{"title":"The draft genome of Corchorus olitorius cv. JRO-524 (Navin)","authors":"Debabrata Sarkar , Ajay Kumar Mahato , Pratik Satya , Avijit Kundu , Sangeeta Singh , Pawan Kumar Jayaswal , Akshay Singh , Kaushlendra Bahadur , Sasmita Pattnaik , Nisha Singh , Avrajit Chakraborty , Nur Alam Mandal , Debajeet Das , Tista Basu , Amitha Mithra Sevanthi , Dipnarayan Saha , Subhojit Datta , Chandan Sourav Kar , Jiban Mitra , Karabi Datta , Nagendra Kumar Singh","doi":"10.1016/j.gdata.2017.05.007","DOIUrl":"10.1016/j.gdata.2017.05.007","url":null,"abstract":"<div><p>Here, we present the draft genome (377.3<!--> <!-->Mbp) of <em>Corchorus olitorious</em> cv. JRO-524 (Navin), which is a leading dark jute variety developed from a cross between African (cv. Sudan Green) and indigenous (cv. JRO-632) types. We predicted from the draft genome a total of 57,087 protein-coding genes with annotated functions. We identified a large number of 1765 disease resistance-like and defense response genes in the jute genome. The annotated genes showed the highest sequence similarities with that of <em>Theobroma cacao</em> followed by <em>Gossypium raimondii</em>. Seven chromosome-scale genetically anchored pseudomolecules were constructed with a total size of 8.53<!--> <!-->Mbp and used for synteny analyses with the cocoa and cotton genomes. Like other plant species, <em>gypsy</em> and <em>copia</em> retrotransposons were the most abundant classes of repeat elements in jute. The raw data of our study are available in SRA database of NCBI with accession number SRX1506532. The genome sequence has been deposited at DDBJ/EMBL/GenBank under the accession LLWS00000000, and the version described in this paper will be the first version (LLWS01000000).</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 151-154"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.05.007","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35024313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.03.008
Galarza Juan A. , Kishor Dhaygude , Johanna Mappes
In this paper we report the public availability of transcriptome resources for the aposematic wood tiger moth (Parasemia plantaginis). A comprehensive assembly methods, quality statistics, and annotation are provided. This reference transcriptome may serve as a useful resource for investigating functional gene activity in aposematic Lepidopteran species. All data is freely available at the European Nucleotide Archive (http://www.ebi.ac.uk/ena) under study accession number: PRJEB14172.
{"title":"De novo transcriptome assembly and its annotation for the aposematic wood tiger moth (Parasemia plantaginis)","authors":"Galarza Juan A. , Kishor Dhaygude , Johanna Mappes","doi":"10.1016/j.gdata.2017.03.008","DOIUrl":"10.1016/j.gdata.2017.03.008","url":null,"abstract":"<div><p>In this paper we report the public availability of transcriptome resources for the aposematic wood tiger moth (<em>Parasemia plantaginis</em>). A comprehensive assembly methods, quality statistics, and annotation are provided. This reference transcriptome may serve as a useful resource for investigating functional gene activity in aposematic Lepidopteran species. All data is freely available at the European Nucleotide Archive (<span>http://www.ebi.ac.uk/ena</span><svg><path></path></svg>) under study accession number: PRJEB14172.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 71-73"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.03.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34892887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-06-01DOI: 10.1016/j.gdata.2017.02.014
Fanchang Zeng , Chaofan Wang , Guirong Zhang , Junmei Wei , Carl A. Bradley , Ray Ming
Fungi are the causal agents of many of the world's most serious plant diseases causing disastrous consequences for large-scale agricultural production. Pathogenicity genomic basis is complex in fungi as multicellular eukaryotic pathogens. The fungus Cercospora sojina is a plant pathogen that threatens global soybean supplies. Here, we report the genome sequence of C. sojina strain S9 and detect genome features and predicted genomic elements. The genome sequence of C. sojina is a valuable resource with potential in studying the fungal pathogenicity and soybean host resistance to frogeye leaf spot (FLS), which is caused by C. sojina. The C. sojina genome sequence has been deposited and available at DDBJ/EMBL/GenBank under the project accession number AHPQ00000000.
{"title":"Draft genome sequence of Cercospora sojina isolate S9, a fungus causing frogeye leaf spot (FLS) disease of soybean","authors":"Fanchang Zeng , Chaofan Wang , Guirong Zhang , Junmei Wei , Carl A. Bradley , Ray Ming","doi":"10.1016/j.gdata.2017.02.014","DOIUrl":"10.1016/j.gdata.2017.02.014","url":null,"abstract":"<div><p>Fungi are the causal agents of many of the world's most serious plant diseases causing disastrous consequences for large-scale agricultural production. Pathogenicity genomic basis is complex in fungi as multicellular eukaryotic pathogens. The fungus <em>Cercospora sojina</em> is a plant pathogen that threatens global soybean supplies. Here, we report the genome sequence of <em>C</em>. <em>sojina</em> strain S9 and detect genome features and predicted genomic elements. The genome sequence of <em>C</em>. <em>sojina</em> is a valuable resource with potential in studying the fungal pathogenicity and soybean host resistance to frogeye leaf spot (FLS), which is caused by <em>C</em>. <em>sojina</em>. The <em>C</em>. <em>sojina</em> genome sequence has been deposited and available at DDBJ/EMBL/GenBank under the project accession number AHPQ00000000.</p></div>","PeriodicalId":56340,"journal":{"name":"Genomics Data","volume":"12 ","pages":"Pages 79-80"},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gdata.2017.02.014","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34892890","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}